Fig. 6
From: Expansion of mouse castration-resistant intermediate prostate stem cells in vitro
AR translocation between the nucleus and cytoplasm. WT CRIPSCs (P25, 6 months) were cultured in the media supplemented with different concentrations of DHT for 12 days (A, 0 nM; C, 0.1 nM; E, 1 nM) or 10 days of low DHT followed by two days of 10 nM DHT (B, D, and F). DAPI-stained nuclei. Scale bars, 100 μm